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Changing the traumatized patient'memory with Prolonged Exposure Therapy

Post-exposure retrieval in the traumatized patient - --: --

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6msdqt
Enrollment
Unknown
Registered
2019-03-04
Start date
2014-09-15
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-traumatic stress condition

Interventions

Patients with Post-Traumatic Stress Disorder (PTSD) had either their traumatic (n = 21) or a neutral (n = 21) memory retrieved 1 hour before a Prolonged Exposure session for two consecutive days. One
Behavioural

Sponsors

Fundação de Amparo à Pesquisa do Estado de São Paulo
Lead Sponsor
Fundação de Amparo à Pesquisa do Estado de São Paulo
Collaborator

Eligibility

Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Meet the DSM-IV criteria for PTSD according to the Structured Clinical Interview for DSM Axis I Disorders, Patient Edition (SCID-I/P); being able to report the traumatic event; have emotional reactivity to trauma recall, defined as a minimum score of 40 in the Visual Analogue Scales (VASs) after describing the traumatic event; have regular menstrual cycle (female patients who were then tested in the follicular phase, defined as the first half of their usual cycle) or were taking hormonal contraceptive.

Exclusion criteria

Exclusion criteria: Patients were excluded if they had any medical condition that could threaten their safety, such as heart or neurological conditions, or current suicide risk; fulfill criteria for bipolar, psychotic, or substance use disorders; were in use of medications known to affect memory reconsolidation or extinction, such as beta-adrenergic blockers, benzodiazepines and anticonvulsants; current pregnancy; and previous participation in another study that could affect the present one.

Design outcomes

Primary

MeasureTime frame
It was expected that the traumatic retrieval group would present greater diminishing in skin conductance responses, compared to the neutral retrieval group. The hyphotesis was confirmed by a statiscal model of Multiple Linear Regression, indicating that the group significantly predicted the outcome: ? = -.31, b = .58, adjusted p-value = .024, CI 95% = -.60 – -.04.

Secondary

MeasureTime frame
It was expected to observe larger decrease in subjective resposes [by the scores of the following instruments, adapted for state version: Visual Analogic Scale, Davidson Traumatic Scale, Impact of Event Scale, Hamilton Depressiom Scale, Profile of Moods Scale and State-Trait Inventory for Anxiety (state version] in the traumatical retrieal group, compared to the neutral retrieval group. This hyphotesis was not confirmed. It could not be observed any diference between the groups, that could be signaled as statistically significant (p > 0.05)

Countries

Brazil

Contacts

Public ContactFelipe;Francisco Corchs;Neto

Instituto de Psiquiatria da Faculdade de Medicina da Universidade de São Paulo;Fapesp

felipe.corchs@gmail.com;franciscolotufo@gmail.com+55-011-30696988;(11) 30697925

Outcome results

None listed

Source: REBEC (via WHO ICTRP)